Indazole-3-carbaldehyde

Details

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Internal ID a7477ad7-aeaa-4c3c-884d-95f8d021d55f
Taxonomy Organoheterocyclic compounds > Benzopyrazoles > Indazoles
IUPAC Name 2H-indazole-3-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H6N2O/c11-5-8-6-3-1-2-4-7(6)9-10-8/h1-5H,(H,9,10)
InChI Key VXOSGHMXAYBBBB-UHFFFAOYSA-N
Popularity 18 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6N2O
Molecular Weight 146.15 g/mol
Exact Mass 146.048012819 g/mol
Topological Polar Surface Area (TPSA) 45.80 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.38
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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5235-10-9
1H-Indazole-3-carboxaldehyde
2H-Indazole-3-carboxaldehyde
2H-indazole-3-carbaldehyde
3-Indazolecarbaldehyde
89939-16-2
indazole-3-carbaldehyde
3-FORMYLINDAZOLE
MFCD04972468
1H-Indazole-3-carboxyaldehyde
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Indazole-3-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.7900 79.00%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.5885 58.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9331 93.31%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8904 89.04%
P-glycoprotein inhibitior - 0.9860 98.60%
P-glycoprotein substrate - 0.9714 97.14%
CYP3A4 substrate - 0.6231 62.31%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8299 82.99%
CYP3A4 inhibition - 0.7287 72.87%
CYP2C9 inhibition - 0.9314 93.14%
CYP2C19 inhibition - 0.8878 88.78%
CYP2D6 inhibition - 0.8327 83.27%
CYP1A2 inhibition + 0.7807 78.07%
CYP2C8 inhibition - 0.7516 75.16%
CYP inhibitory promiscuity - 0.7876 78.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6950 69.50%
Eye corrosion - 0.9908 99.08%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.5409 54.09%
Skin corrosion - 0.9520 95.20%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7743 77.43%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.8074 80.74%
skin sensitisation - 0.8644 86.44%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.5426 54.26%
Acute Oral Toxicity (c) III 0.8027 80.27%
Estrogen receptor binding - 0.8817 88.17%
Androgen receptor binding - 0.7983 79.83%
Thyroid receptor binding - 0.6432 64.32%
Glucocorticoid receptor binding - 0.8781 87.81%
Aromatase binding - 0.6765 67.65%
PPAR gamma - 0.5122 51.22%
Honey bee toxicity - 0.8771 87.71%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity - 0.5828 58.28%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.37% 95.56%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 91.46% 96.47%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.82% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 83.18% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.35% 94.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.07% 99.23%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 11367068
LOTUS LTS0148130
wikiData Q72482782